Compliance Specialist (f/m/d)

Compliance Specialist (f/m/d)

Randstad Deutschland GmbH & Co. KG

Mainz am Rhein
Penzberg
GxP compliance
clinical trial supply management
project-related GxP documentation
quality standards (GMP, GCP, GDP)
MS Office applications

Hexjobs Insights

Position: Compliance Specialist at Roche in Penzberg. Responsibilities include GxP compliance support, documentation, operational tasks, and process optimization. Requirements: University degree, experience in pharma/biotech, language skills.

Schlüsselwörter

GxP compliance
clinical trial supply management
project-related GxP documentation
quality standards (GMP, GCP, GDP)
MS Office applications

Vorteile

  • tariff-based wages
  • care by a company medical center
  • employee discounts
  • up to 30 days vacation per year
  • extensive social benefits including Christmas and holiday bonuses
  • definition of career goals
  • candid corporate culture

Firmenbeschreibung

Good jobs with fair wages are rare, you say? Well, today is your lucky day! Our subsidiary Randstad professional solutions has a vacant position as compliance specialist at the pharmaceutical company Roche in Penzberg. Tariff-based wages, care by a company medical center, and employee discounts - all advantages that you can count on with Randstad. It's best to apply online right away and secure this job! Applications from individuals with disabilities are warmly welcome.

Ihre Aufgaben

  • Support GxP compliance of all activities in the clinical trial supply management, drug-related distribution and storage
  • Responsibility for the project-related GxP documentation and maintenance of lists
  • Operational support and independent performance of operational tasks as process expert in the IMP GxP Compliance Team across diverse clinical trials and R&D Programs (e.g. Batch Record Reviews and TMF Filing)
  • Establish and maintain inspection readiness for clinical trial supply activities and support in preparing, accompanying and following up on audits and inspections
  • Optimization of processes and workflows (e.g. support in the creation and review of SOPs and other GxP related documents)

Unsere Anforderungen

  • Completed university degree or a similar education with a scientific focus
  • Several years of work experience in the pharmaceutical or biotech industry
  • Knowledge of quality standards (GMP, GCP, GDP) and regulatory requirements in an international environment
  • Profound skills in the use of MS Office applications and a quality management system
  • Strong communications skills, good German language skills and fluency in English

Das dürfen Sie erwarten

  • Performance-based salary package depending on qualifications and professional experience
  • Up to 30 days vacation per year
  • Extensive social benefits, incl. Christmas and holiday bonuses
  • Definition of career goals
  • Candid corporate culture
Aufrufe: 7
Veröffentlichtvor 22 Tagen
Läuft abin 7 Tagen
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